Torthaí cuardaigh - Ian Glass
- 1 - 20 toradh as 59 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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1
X linked mental retardation. de réir Ian Glass
Foilsithe / Cruthaithe 1991Revisão -
2
Joubert syndrome (and related disorders) (OMIM 213300) de réir Melissa A. Parisi, Dan Doherty, Phillip F. Chance, Ian Glass
Foilsithe / Cruthaithe 2007Artigo -
3
PI3K-Yap activity drives cortical gyrification and hydrocephalus in mice de réir Achira Roy, Rory Murphy, Mei Deng, James W. MacDonald, Theo K. Bammler, Kimberly A. Aldinger, Ian Glass, Kathleen J. Millen
Foilsithe / Cruthaithe 2019Artigo -
4
Chromosomal instability in human trophoblast stem cells and placentas de réir Danyang Wang, Andrew Cearlock, Katherine Lane, Chongchong Xu, Ian Jan, Stephen A. McCartney, Ian Glass, Rajiv C. McCoy, Min Yang
Foilsithe / Cruthaithe 2025Artigo -
5
The NPHP1 Gene Deletion Associated with Juvenile Nephronophthisis Is Present in a Subset of Individuals with Joubert Syndrome de réir Melissa A. Parisi, Craig L. Bennett, Melissa Eckert, William B. Dobyns, Joseph G. Gleeson, Dennis Shaw, Ruth McDonald, Allison A. Eddy, Phillip F. Chance, Ian Glass
Foilsithe / Cruthaithe 2004Artigo -
6
Direct Diagnosis of Myotonic Dystrophy with a Disease-Specific DNA Marker de réir Peggy Shelbourne, June Davies, Jessica L. Buxton, Maria Anvret, Elisabeth Blennow, M Bonduelle, Eric Schmedding, Ian Glass, R H Lindenbaum, Russell J.M. Lane, Robert Williamson, Keith Johnson
Foilsithe / Cruthaithe 1993Artigo -
7
Differentiation of Human Intestinal Organoids with Endogenous Vascular Endothelial Cells de réir Emily M. Holloway, Joshua H. Wu, Michael Czerwinski, Caden W. Sweet, Angeline Wu, Yu-Hwai Tsai, Sha Huang, Amy E. Stoddard, Meghan M. Capeling, Ian Glass, Jason R. Spence
Foilsithe / Cruthaithe 2020Artigo -
8
Mutation analysis of NPHP6/CEP290 in patients with Joubert syndrome and Senior Loken syndrome de réir Josiane Hélou, Edgar A. Otto, Massimo Attanasio, S. J. Allen, Melissa A. Parisi, Ian Glass, Boris Utsch, S. Hashmi, Elisa Fazzi, Heymut Omran, John F. O’Toole, John A. Sayer, Friedhelm Hildebrandt
Foilsithe / Cruthaithe 2007Carta -
9
A Report of Dizygous Monochorionic Twins de réir Vivienne Souter, Raj P. Kapur, Dale R. Nyholt, Kristen J. Skogerboe, David Myerson, Carl C.T. Ton, Kent E. Opheim, Thomas R. Easterling, Laurence E. Shields, Grant W. Montgomery, Ian Glass
Foilsithe / Cruthaithe 2003Artigo -
10
Rhombencephalosynapsis: a hindbrain malformation associated with incomplete separation of midbrain and forebrain, hydrocephalus and a broad spectrum of severity de réir Gisele E. Ishak, Jennifer C. Dempsey, Dennis Shaw, Hannah M. Tully, Margaret P Adam, Pedro A. Sanchez‐Lara, Ian Glass, Tessa Rue, Kathleen J. Millen, William B. Dobyns, Dan Doherty
Foilsithe / Cruthaithe 2012Artigo -
11
Single-Cell Transcriptomic Comparison of Human Fetal Retina, hPSC-Derived Retinal Organoids, and Long-Term Retinal Cultures de réir Akshayalakshmi Sridhar, Akina Hoshino, Connor Finkbeiner, Alex Chitsazan, Li Dai, Alexandra K. Haugan, Kayla M. Eschenbacher, Dana L. Jackson, Cole Trapnell, Olivia Bermingham‐McDonogh, Ian Glass, Thomas A. Reh
Foilsithe / Cruthaithe 2020Artigo -
12
In Vitro and In Vivo Development of the Human Airway at Single-Cell Resolution de réir Alyssa J. Miller, Qianhui Yu, Michael Czerwinski, Yu-Hwai Tsai, Renee F. Conway, Angeline Wu, Emily M. Holloway, Taylor Walker, Ian Glass, Barbara Treutlein, J. Gray Camp, Jason R. Spence
Foilsithe / Cruthaithe 2020Artigo -
13
Joubert Syndrome: Ophthalmological Findings in Correlation with Genotype and Hepatorenal Disease in 99 Patients Prospectively Evaluated at a Single Center de réir Brian P. Brooks, Wadih M. Zein, A. Thompson, Maryam Mokhtarzadeh, Dan Doherty, Melissa A. Parisi, Ian Glass, May Christine V. Malicdan, Thierry Vilboux, Meghana Vemulapalli, James C. Mullikin, William A. Gahl, Meral Gunay‐Aygun
Foilsithe / Cruthaithe 2018Artigo -
14
Aberrant Drp1-mediated mitochondrial division presents in humans with variable outcomes de réir Brittany N. Whitley, Christina Lam, Hong Cui, Katrina Haude, Renkui Bai, Luis Escobar, Afifa Hamilton, Lauren Brady, Mark A. Tarnopolsky, Lauren Dengle, Jonathan Picker, Sharyn A. Lincoln, Laura L. Lackner, Ian Glass, Suzanne Hoppins
Foilsithe / Cruthaithe 2018Artigo -
15
Mapping Development of the Human Intestinal Niche at Single-Cell Resolution de réir Emily M. Holloway, Michael Czerwinski, Yu-Hwai Tsai, Joshua H. Wu, Angeline Wu, Charlie J. Childs, Katherine D. Walton, Caden W. Sweet, Qianhui Yu, Ian Glass, Barbara Treutlein, J. Gray Camp, Jason R. Spence
Foilsithe / Cruthaithe 2020Artigo -
16
Mutations in TRAPPC12 Manifest in Progressive Childhood Encephalopathy and Golgi Dysfunction de réir Miroslav P. Milev, Megan E. Grout, Djenann Saint‐Dic, Yong-Han Hank Cheng, Ian Glass, Christopher J. Hale, D. Hanna, Michael O. Dorschner, Keshika Prematilake, Avraham Shaag, Orly Elpeleg, Michael Sacher, Dan Doherty, Simon Edvardson
Foilsithe / Cruthaithe 2017Artigo -
17
R-SPONDIN2 mesenchymal cells form the bud tip progenitor niche during human lung development de réir Renee Hein, Joshua H. Wu, Emily M. Holloway, Tristan Frum, Ansley S. Conchola, Yu-Hwai Tsai, Angeline Wu, Alexis S. Fine, Alyssa J. Miller, Emmanuelle Szenker‐Ravi, Kelley S. Yan, Calvin J. Kuo, Ian Glass, Bruno Reversade, Jason R. Spence
Foilsithe / Cruthaithe 2022Artigo -
18
Retinoic acid signaling regulates spatiotemporal specification of human green and red cones de réir Sarah E. Hadyniak, Joanna F. D. Hagen, Kiara C. Eldred, Boris Brenerman, Katarzyna A. Hussey, Rajiv C. McCoy, Michael Sauria, James A. Kuchenbecker, Thomas A. Reh, Ian Glass, Maureen Neitz, Jay Neitz, James Taylor, Robert J. Johnston
Foilsithe / Cruthaithe 2024Artigo -
19
The Molecular Basis of X-Linked Spondyloepiphyseal Dysplasia Tarda de réir Ági K. Gedeon, George E. Tiller, M. Le Merrer, S. Heuertz, Lisbeth Tranebjærg, David Chitayat, Stephen P. Robertson, Ian Glass, Ravi Savarirayan, William G. Cole, David L. Rimoin, Boris G. Kousseff, Hirofumi Ohashi, Bernhard Zabel, Arnold Münnich, Jozef Gécz, John C. Mulley
Foilsithe / Cruthaithe 2001Artigo -
20
Prospective Evaluation of Kidney Disease in Joubert Syndrome de réir Leah R. Fleming, Daniel Doherty, Melissa A. Parisi, Ian Glass, Joy Bryant, Roxanne Fischer, Barış Türkbey, Peter L. Choyke, Kailash Daryanani, Meghana Vemulapalli, James C. Mullikin, May Christine V. Malicdan, Thierry Vilboux, John A. Sayer, William A. Gahl, Meral Gunay‐Aygun
Foilsithe / Cruthaithe 2017Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Genetics
Gene
Cell biology
Medicine
Neuroscience
Phenotype
Joubert syndrome
Computational biology
Internal medicine
Stem cell
Pathology
Cilium
Gene expression
Mutation
Anatomy
Ciliopathy
Genome
Immunology
Progenitor cell
Cerebellum
Transcriptome
Biochemistry
Cell
Disease
Exome sequencing
Transcription factor
Endocrinology
Fetus
Organoid